Astral Medical Systems
FDA Regulatory Profile
Astral Medical Systems appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 12, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K900506 | MODIFIED COATRON II AND COATRON JR. | March 12, 1990 |
| K851153 | COATRON F(SAME AS COATRON, BUT ALSO DOES FIBRINOGE | November 5, 1985 |
| K853734 | APOLLO DENSITOMETER | September 25, 1985 |
| K851154 | ELECTROPHORESIS APPARATUS, FOR CLINICAL USE 160,18 | May 13, 1985 |